Болеста на Фабри-Андерсон е ретко метаболно Х-врзано наследно заболување, кое се карактеризира со наталожување на неразложените масти (глобо-триаозилцерамиди Гб-3) во клетките насекаде низ човековото тело, поради недостаток или отсуство на ензимот алфа-галактозидаза. Директорот на Клиниката за Нефрологија, Никола Ѓорѓиевски со стручно предавање на оваа тема со цел подигнување на јавната свест за ова заболување
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